Humira

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

adalimumab

Available from:

AbbVie Deutschland GmbH Co. KG

ATC code:

L04AB04

INN (International Name):

adalimumab

Therapeutic group:

Immunosoppressanti

Therapeutic area:

Spondylitis, Ankylosing; Arthritis, Juvenile Rheumatoid; Uveitis; Colitis, Ulcerative; Psoriasis; Arthritis, Psoriatic; Crohn Disease; Arthritis, Rheumatoid

Therapeutic indications:

Jekk jogħġbok irreferi għad-dokument ta 'informazzjoni dwar il-prodott.

Product summary:

Revision: 89

Authorization status:

Awtorizzat

Authorization date:

2003-09-08

Patient Information leaflet

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM TAL-PRODOTT MEDIĊINALI
Humira 20mg soluzzjoni għall-injezzjoni f’siringa mimlija
għal-lest
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull siringa mimlija għal-lest b’doża waħda ta’ 0.2 ml fiha 20
mg adalimumab.
Adalimumab huwa anti-korp uman monoklonali rikombinanti prodott
fiċ-ċelluli ta’ l-ovarji tal-
ħamster ċiniż.
Għal-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Soluzzjoni għall-injezzjoni (injezzjoni)
Soluzzjoni ċara, bla kulur.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Artrite idjopatika taż-żagħżagħ
_Artrite idjopatika poliartikulari taż-żagħżagħ_
Humira meta jingħata flimkien ma’ methotrexate huwa ndikat
għall-kura ta’ artrite attiva idjopatika
poliartikulari taż-żagħżagħ, f’pazjenti li għandhom sentejn
jew aktar, li ma kellhomx rispons kif
mistenni għal kura b’mediċini anti-rewmatiċi li jaffetwaw
il-proċess tal-mard (DMARDs). Humira
jista’ jingħata waħdu f’każ ta’ intolleranza għal
methotrexate, jew f’każ li t-tkomplija tal-kura
b’methotrexate ma tkunx tajba (għall-effikaċja ta’ meta
jingħata waħdu ara sezzjoni 5.1). Użu ta’
Humira ma ġiex studjat f’pazjenti li għandhom anqas minn sentejn.
_Artrite relata mal-entesite_
Humira huwa ndikat għall-kura ta’ artrite attiva relatata
mal-entesite f’pazjenti, ta’ 6 snin jew akbar, li
kellhom rispons inadegwat għal, jew li ma jitollerawx, terapija
konvenzjonali (ara sezzjoni 5.1).
Psorjasi tal-plakka pedjatrika
Humira huwa ndikat għat-trattament ta’ psorjasi tal-plakka severa u
kronika fit-tfal u adoloxxenti
minn 4 snin il-fuq u li kellhom rispons mhux adegwat jew huma
kandidati mhux xierqa għat-terapija
topika u fototerapiji.
Il-marda _Crohn (Crohn’s diease) _fit-tfal
Humira huwa ndikat għall-kura tal-marda _Crohn (Crohn’s diease)
_attiva minn moderata sa severa fit-
tfal (minn 6 snin il-fuq) li ma kellhomx rispons kif mistenni
għall-kura konvenzjonali in
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM TAL-PRODOTT MEDIĊINALI
Humira 20mg soluzzjoni għall-injezzjoni f’siringa mimlija
għal-lest
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Kull siringa mimlija għal-lest b’doża waħda ta’ 0.2 ml fiha 20
mg adalimumab.
Adalimumab huwa anti-korp uman monoklonali rikombinanti prodott
fiċ-ċelluli ta’ l-ovarji tal-
ħamster ċiniż.
Għal-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Soluzzjoni għall-injezzjoni (injezzjoni)
Soluzzjoni ċara, bla kulur.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Artrite idjopatika taż-żagħżagħ
_Artrite idjopatika poliartikulari taż-żagħżagħ_
Humira meta jingħata flimkien ma’ methotrexate huwa ndikat
għall-kura ta’ artrite attiva idjopatika
poliartikulari taż-żagħżagħ, f’pazjenti li għandhom sentejn
jew aktar, li ma kellhomx rispons kif
mistenni għal kura b’mediċini anti-rewmatiċi li jaffetwaw
il-proċess tal-mard (DMARDs). Humira
jista’ jingħata waħdu f’każ ta’ intolleranza għal
methotrexate, jew f’każ li t-tkomplija tal-kura
b’methotrexate ma tkunx tajba (għall-effikaċja ta’ meta
jingħata waħdu ara sezzjoni 5.1). Użu ta’
Humira ma ġiex studjat f’pazjenti li għandhom anqas minn sentejn.
_Artrite relata mal-entesite_
Humira huwa ndikat għall-kura ta’ artrite attiva relatata
mal-entesite f’pazjenti, ta’ 6 snin jew akbar, li
kellhom rispons inadegwat għal, jew li ma jitollerawx, terapija
konvenzjonali (ara sezzjoni 5.1).
Psorjasi tal-plakka pedjatrika
Humira huwa ndikat għat-trattament ta’ psorjasi tal-plakka severa u
kronika fit-tfal u adoloxxenti
minn 4 snin il-fuq u li kellhom rispons mhux adegwat jew huma
kandidati mhux xierqa għat-terapija
topika u fototerapiji.
Il-marda _Crohn (Crohn’s diease) _fit-tfal
Humira huwa ndikat għall-kura tal-marda _Crohn (Crohn’s diease)
_attiva minn moderata sa severa fit-
tfal (minn 6 snin il-fuq) li ma kellhomx rispons kif mistenni
għall-kura konvenzjonali in
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 11-10-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 11-10-2022
Public Assessment Report Public Assessment Report Bulgarian 09-12-2020
Patient Information leaflet Patient Information leaflet Spanish 11-10-2022
Public Assessment Report Public Assessment Report Spanish 09-12-2020
Patient Information leaflet Patient Information leaflet Czech 11-10-2022
Public Assessment Report Public Assessment Report Czech 09-12-2020
Patient Information leaflet Patient Information leaflet Danish 11-10-2022
Public Assessment Report Public Assessment Report Danish 09-12-2020
Patient Information leaflet Patient Information leaflet German 11-10-2022
Public Assessment Report Public Assessment Report German 09-12-2020
Patient Information leaflet Patient Information leaflet Estonian 11-10-2022
Public Assessment Report Public Assessment Report Estonian 09-12-2020
Patient Information leaflet Patient Information leaflet Greek 11-10-2022
Public Assessment Report Public Assessment Report Greek 09-12-2020
Patient Information leaflet Patient Information leaflet English 11-10-2022
Public Assessment Report Public Assessment Report English 09-12-2020
Patient Information leaflet Patient Information leaflet French 11-10-2022
Public Assessment Report Public Assessment Report French 09-12-2020
Patient Information leaflet Patient Information leaflet Italian 11-10-2022
Public Assessment Report Public Assessment Report Italian 09-12-2020
Patient Information leaflet Patient Information leaflet Latvian 11-10-2022
Public Assessment Report Public Assessment Report Latvian 09-12-2020
Patient Information leaflet Patient Information leaflet Lithuanian 11-10-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 11-10-2022
Public Assessment Report Public Assessment Report Lithuanian 09-12-2020
Patient Information leaflet Patient Information leaflet Hungarian 11-10-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 11-10-2022
Public Assessment Report Public Assessment Report Hungarian 09-12-2020
Patient Information leaflet Patient Information leaflet Dutch 11-10-2022
Public Assessment Report Public Assessment Report Dutch 09-12-2020
Patient Information leaflet Patient Information leaflet Polish 11-10-2022
Public Assessment Report Public Assessment Report Polish 09-12-2020
Patient Information leaflet Patient Information leaflet Portuguese 11-10-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 11-10-2022
Public Assessment Report Public Assessment Report Portuguese 09-12-2020
Patient Information leaflet Patient Information leaflet Romanian 11-10-2022
Public Assessment Report Public Assessment Report Romanian 09-12-2020
Patient Information leaflet Patient Information leaflet Slovak 11-10-2022
Public Assessment Report Public Assessment Report Slovak 09-12-2020
Patient Information leaflet Patient Information leaflet Slovenian 11-10-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 11-10-2022
Public Assessment Report Public Assessment Report Slovenian 09-12-2020
Patient Information leaflet Patient Information leaflet Finnish 11-10-2022
Public Assessment Report Public Assessment Report Finnish 09-12-2020
Patient Information leaflet Patient Information leaflet Swedish 11-10-2022
Public Assessment Report Public Assessment Report Swedish 09-12-2020
Patient Information leaflet Patient Information leaflet Norwegian 11-10-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 11-10-2022
Patient Information leaflet Patient Information leaflet Icelandic 11-10-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 11-10-2022
Patient Information leaflet Patient Information leaflet Croatian 11-10-2022
Public Assessment Report Public Assessment Report Croatian 09-12-2020

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